memory impairment Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An impairment of memory as manifested by a reduced ability to remember things such as dates and names, and increased forgetfulness. (Human Phenotype Ontology, HP_0002354)
External Link
Similar Terms
Downloads & Tools


19 genes associated with the memory impairment phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
CAMTA1 calmodulin binding transcription activator 1 1.26545
CTNNBL1 catenin, beta like 1 1.16319
WWC1 WW and C2 domain containing 1 0.942765
TTC21B tetratricopeptide repeat domain 21B 0.942765
P2RY6 pyrimidinergic receptor P2Y, G-protein coupled, 6 0.855449
PPARG peroxisome proliferator-activated receptor gamma 0.853087
SCN1A sodium channel, voltage gated, type I alpha subunit 0.844241
TBC1D8 TBC1 domain family, member 8 (with GRAM domain) 0.772842
GFRA1 GDNF family receptor alpha 1 0.714661
SPOCK1 sparc/osteonectin, cwcv and kazal-like domains proteoglycan (testican) 1 0.656743
COX6C cytochrome c oxidase subunit VIc 0.649599
KHDRBS2 KH domain containing, RNA binding, signal transduction associated 2 0.635284
DEPDC5 DEP domain containing 5 0.626701
ZDHHC3 zinc finger, DHHC-type containing 3 0.624663
FOXF1 forkhead box F1 0.616892
ZNF638 zinc finger protein 638 0.604135
FAM19A5 family with sequence similarity 19 (chemokine (C-C motif)-like), member A5 0.604135
RREB1 ras responsive element binding protein 1 0.591289
LRRC4C leucine rich repeat containing 4C 0.57836